Canonical Allele Identifier: CA1727580303

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189377G= , CM000669.2:g.96189377G=	GRCh38
NC_000007.13:g.95818689G= , CM000669.1:g.95818689G=	GRCh37
NC_000007.12:g.95656625G=	NCBI36
NG_012247.1:g.137771C=
NG_012247.2:g.137771C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.850C= MANE Select	ENSP00000265631.6:p.Arg284=
ENST00000265631.9:c.850C=	ENSP00000265631.5:p.Arg284=
ENST00000416240.6:c.850C=	ENSP00000400101.2:p.Arg284=
ENST00000484495.5:n.3C=
NM_001160210.1:c.850C=	NP_001153682.1:p.Arg284=
NM_014251.2:c.850C=	NP_055066.1:p.Arg284=
NR_027662.1:n.925C=
XM_006715831.2:c.883C=	XP_006715894.1:p.Arg295=
XM_011515727.1:c.883C=	XP_011514029.1:p.Arg295=
XM_011515728.1:c.-3C=	XP_011514030.1:n.-3C=
XM_006715831.4:c.883C=	XP_006715894.1:p.Arg295=
XM_011515727.3:c.883C=	XP_011514029.1:p.Arg295=
XM_017011663.1:c.841C=	XP_016867152.1:p.Arg281=
XM_017011664.2:c.-3C=	XP_016867153.1:n.-3C=
XM_017011665.1:c.-3C=	XP_016867154.1:n.-3C=
XR_001744525.2:n.1021C=
XR_002956405.1:n.1163C=
NM_014251.3:c.850C= MANE Select	NP_055066.1:p.Arg284=
NR_027662.2:n.876C=
NM_001160210.2:c.850C=	NP_001153682.1:p.Arg284=